Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

RISK aversion in Italian forensic and non-forensic patients with schizophrenia spectrum disorders

  • Nicola Canessa ,

    Contributed equally to this work with: Nicola Canessa, Laura Iozzino

    Roles Conceptualization, Data curation, Investigation, Writing – original draft

    Affiliations IUSS Cognitive Neuroscience (ICON) Center, Scuola Universitaria Superiore IUSS, Pavia, Italy, Istituti Clinici Scientifici Maugeri IRCCS, Cognitive Neuroscience Laboratory of Pavia Institute, Pavia, Italy

  • Laura Iozzino ,

    Contributed equally to this work with: Nicola Canessa, Laura Iozzino

    Roles Conceptualization, Data curation, Writing – original draft

    Affiliation IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Unit of Epidemiological Psychiatry and Evaluation, Brescia, Italy

  • Sonia Andreose,

    Roles Writing – original draft

    Affiliation IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Psychiatric Unit, Brescia, Italy

  • Luca Castelletti,

    Roles Writing – original draft

    Affiliation REMS del Veneto, ULSS9 Scaligera, Verona, Italy

  • Giovanni Conte,

    Roles Writing – original draft

    Affiliation Department of Mental Health, ASST di Brescia, Brescia, Italy

  • Alexander Dvorak,

    Roles Writing – original draft

    Affiliation Justizanstalt Goellersdorf, Göllersdorf, Austria

  • Clarissa Ferrari,

    Roles Formal analysis, Methodology, Writing – original draft

    Affiliation IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Unit of Statistics, Brescia, Italy

  • Janusz Heitzman,

    Roles Conceptualization, Writing – original draft

    Affiliation Institute of Psychiatry and Neurology, Department of Forensic Psychiatry, Warsaw, Poland

  • Ambra Macis,

    Roles Formal analysis, Methodology, Writing – original draft

    Affiliation IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Unit of Statistics, Brescia, Italy

  • Inga Markiewicz,

    Roles Writing – original draft

    Affiliation Institute of Psychiatry and Neurology, Department of Forensic Psychiatry, Warsaw, Poland

  • Giulia Mattavelli,

    Roles Writing – original draft

    Affiliations IUSS Cognitive Neuroscience (ICON) Center, Scuola Universitaria Superiore IUSS, Pavia, Italy, Istituti Clinici Scientifici Maugeri IRCCS, Cognitive Neuroscience Laboratory of Pavia Institute, Pavia, Italy

  • Giuseppe Nicolò,

    Roles Writing – original draft

    Affiliation REMS Minerva, Department of Mental Health, ASL Roma 5, Rome, Italy

  • Marco Picchioni,

    Roles Conceptualization, Writing – original draft

    Affiliations Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, United Kingdom, St Magnus Hospital, Surrey, United Kingdom

  • Giuseppe Restuccia,

    Roles Writing – original draft

    Affiliation REMS di Volterra, Azienda USL Toscana Nord Ovest, Volterra, Italy

  • Gianfranco Rivellini,

    Roles Writing – original draft

    Affiliation REMS del Veneto, ULSS9 Scaligera, Verona, Italy

  • Fabio Teti,

    Roles Writing – original draft

    Affiliation Sistema Polimodulare di REMS Provvisorie, ASST di Mantova, Castiglione delle Stiviere, Italy

  •  [ ... ],
  • Giovanni de Girolamo

    Roles Conceptualization, Funding acquisition, Writing – original draft

    gdegirolamo@fatebenefratelli.eu

    Affiliation IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Unit of Epidemiological Psychiatry and Evaluation, Brescia, Italy

  • [ view all ]
  • [ view less ]

Abstract

Background

Goal-directed decision-making is a central component of the broader reward and motivation system, and requires the ability to dynamically integrate both positive and negative feedback from the environment in order to maximize rewards and minimize losses over time. Altered decision-making processes, in which individuals fail to consider the negative consequences of their decisions on both themselves and others, may play a role in driving antisocial behaviour.

Aim

The main study aim was to investigate possible differences in loss and risk aversion across matched patients, all with a schizophrenia spectrum disorder (SSD), but who varied according to whether they had a history of serious interpersonal violence or not, and a sample of healthy controls with no history of violence.

Results

The sample included 14 forensic and 21 non-forensic patients with SSD, and 41 healthy controls. Among the three decision-making variables under investigation, risk aversion was the only significant predictor of membership of the three groups, with greater risk aversion among non-forensic patients with SSD compared to healthy controls. No differences were observed across groups in loss aversion and choice consistency.

Conclusions

This evidence suggests a new potential treatment target for rehabilitative measures aimed at achieving functional improvements in patients with SSD by selectively leveraging the neuro-cognitive processing of reward.

1. Introduction

Decision-Making is an inherent part of everyday-life, with effects at both individual and societal levels. Understanding the factors that influence decision-making is crucial for social and behavioural sciences, particularly when trying to identify the drivers of aberrant behaviour and violence. In Europe in 2019 there were 642,500 police-recorded assaults, up 11% from 577,400 in 2014 (https://ec.europa.eu/eurostat/web/crime/data/database). Such behaviours might reflect alterations in a key stage of decision-making such as mentally anticipating and evaluating the consequences of one’s own decisions and actions, particularly when they impact on another’s wellbeing.

From a biological perspective, this process involves the coordinated activity of a broad neural network. The fronto-limbic network and ventromedial prefrontal regions process appetitive and aversive stimuli [15], alongside the dorsal sector of the anterior cingulate cortex supporting outcome evaluation and performance monitoring [6], while the fronto-parietal network underpins executive control and behavioural adjustments [79]. Within this framework, individual variations in decision-making can be explained through differential sensitivity to ubiquitous economic trade-offs [10], such as those between probabilistic and certain outcomes, or between prospective gains and losses, and their association with psychological dimensions such as affect, arousal [11] and impulsivity [12]. While the former trade-off highlights risk aversion as the usual preference for certain, definite outcomes compared with probabilistic outcomes [10, 13], the concept of loss aversion reflects the larger psychological impact of anticipating negative, compared with positive, outcomes [4, 10, 14].

Different theoretical models have been proposed to explain the drivers of offenders’ behaviour [15], including the Routine Activity Theory [16], stressing the role of the situational context, or the Rational Choice Theory [17, 18], grounded in individual differences in processing the trade-off between risk versus certainty or immediate versus delayed outcomes. The effect of such variables on decision-making can be assessed using neuro-cognitive tasks capable of detecting differences across normal and pathological conditions that might explain real-life offending behaviour [7, 10]. Indeed, rates of mental disorders are higher among offenders than in the general population, with psychosis, substance use disorder and severe (psychotic) depression showing the highest rates [19, 20]. Despite preliminary evidence of impaired feedback-based learning in offenders [7], however, it is still unclear whether they differ from the general population in terms of risk taking [2124].

Studies based on the Iowa Gambling Task (IGT) highlighted distinct patterns of impaired performance in criminal offenders compared with healthy controls [25], reflecting either hypersensitivity to rewards (i.e., overweighting of potential gains as compared to losses), or heightened sensitivity to immediate outcomes [18].

Importantly, most previous studies have investigated decision-making skills in offenders [24] and people with mental disorders (e.g., Hiser and Koenigs, 2018) [26] separately, thus, largely neglecting the possible combined effects of these factors on decision-making.

We therefore aimed to fill this gap by assessing risk taking in patients with schizophrenia spectrum disorders (SSD) with and without a history of serious forensic offending. Previous studies addressing risk taking in patients with SSD reported partially inconsistent evidence. Impaired IGT performance, in patients with SSD compared with healthy controls [27, 28], was found to reflect increased sensitivity to rewards [29] and the severity of depressive symptoms [30]. previous studies reported both increased [31, 32] and decreased [30, 33] risk aversion in patients with SSD compared to healthy controls, whereas an absence of patients’ loss aversion was reported in two studies [34, 35]. To date, however, well-established economic paradigms for testing loss and risk aversion within a single study [36] have been only employed in a non-clinical sample of untreated individuals displaying negative symptoms and/or hypomania [37], but not in SSD.

On this basis, we investigated possible differences in risk and loss aversion across sex- and age-matched patients with SSD with or without a history of serious interpersonal violence compared to healthy controls with no history of violence, while controlling for differences between the two patient groups in sex, lifetime substance/alcohol use, and education.

2. Materials and methods

2.1 Participants

This study was part of the EUropean VIOlence Risk and MEntal Disorders (EU-VIORMED), a European multicentre case-control study conducted in five countries (Austria, Germany, Italy, Poland and the UK) [38]. For organizational reasons (including issues related to the access to forensic facilities), this decision-making task was only administered to patients recruited in Italian forensic facilities.

The study included three groups: forensic patients with SSD, non-forensic patients with SSD and healthy controls. All patients had a confirmed diagnosis based on chart review of SSD according to DSM-5 (Diagnostic and Statistical Mental Disorders Manual) [39] criteria and were aged between 18 and 65 years. ‘Forensic’ patients were defined as patients with SSD that have committed a homicide, attempted homicide or other assault that caused serious physical injury to another person. They were recruited from forensic institutions.

‘Non-forensic’ patients had a SSD diagnosis, were sex- and age-matched to forensic patients, and had never committed an act of severe violence, as confirmed by medical records and by the treating clinicians. The task was also administered to a sample of healthy controls who had no history of mental disorder and no history of severe interpersonal violence.

Exclusion criteria for all groups included: (a) a diagnosis of intellectual disability; (b) a traumatic brain injury, an organic brain disorder or cancer; (c) inability to speak the national language fluently; and (d) planned discharge in the next month.

2.2 Recruitment

In each study centre, treating clinicians invited participants under their care to enter the study. Participants were provided with written information about the study and had an opportunity to ask questions. Informed consent was also sought to allow to collect information from caregivers, family members or case-managers/clinical staff for additional/missing information.

The recruitment of forensic cases was the priority, with care given to matching criteria (e.g., age categories, sex and diagnosis). This helped in finding matched non-forensic SSD participants, who were recruited from local adult psychiatric services.

The study was approved by the Ethical Committee of IRCCS Centro San Giovanni di Dio Fatebenefratelli (Brescia, Italy; permissions n. 74–2018 and n. 73–2019). All participants gave their written informed consent after a full description of the study aims and methods.

2.3 Socio-demographic, clinical, functional and violence assessment

All participants underwent a multidimensional standardized evaluation. A Patient Information Form (PIF) was used to collect socio-demographic and clinical information. The Index Violence Sheet (IVS) and a Risk Factors Questionnaire (RFQ) were ad-hoc instruments used to collect data about the index violence and violence risk factors for forensic patients (for more details see Supporting Information). The Positive and Negative Syndrome Scale-PANSS [40] was used to evaluate current psychotic symptoms [41, 42]. The Brief Assessment of Cognition in Schizophrenia (BACS) [43] evaluated cognitive functioning. The World Health Organization Disability Assessment Schedule (WHODAS-2.0) [44] was used to assess functioning and disability related to health conditions across six functional domains: cognition, mobility, self-care, getting along, life activities and participation.

2.4 Decision-making assessment

All participants performed a task designed to measure their degree of loss aversion (defined as the overweighting of negative, compared with positive, choice outcomes), and risk aversion (defined as the preference for certain compared to probabilistic outcomes). The former task included 49 trials in which the subjects had to choose between a certain “0” outcome and a lottery/gamble, which might result in a gain (G) or a loss (L) with equal (50–50%) probabilities. G and L changed at every trial, which allowed us to estimate the “loss aversion” (λ) parameter such that λ >1 or <1 indicates loss aversion or loss seeking, respectively. Importantly, the popular claim of an average λ≈215 has been questioned by the evidence of no loss aversion for small to moderate amounts [45, 46]. Risk aversion was assessed with 30 further trials in which the participants were asked to choose between a certain gain (C) and a gamble which, with equal (50–50%) probabilities, might result in a gain G (with G > C) or nothing (0). C and G changed at every trial, which allowed to estimate a “risk aversion” (ρ) parameter reflecting the diminishing marginal sensitivity to probabilistic (i.e., risky) outcomes.

2.5 Statistical analyses: group comparisons

Frequencies and percentages for categorical variables, and means and standard deviations (SDs) for continuous variables, were evaluated. Chi-squared or Fisher’s exact tests were used to compare categorical variables among the groups of interest. The normality assumption for continuous variables distribution was tested through histogram plots and normality tests; coherently, group comparisons were performed by t-tests and ANOVA or the non-parametric Mann-Whitney and Kruskal-Wallis tests according to the nature of the data. Finally, multinomial logistic regression models were used to assess the associations between the three groups (dependent variable) and decision-making variables (independent variables), adjusting for potential confounders. All tests were two-tailed and the significance level was set at 0.05. The analyses were performed using IBM SPSS Statistics for Windows (Version 26.0. Armonk, NY: IBM Corp).

2.6 Extraction of decision-making parameters

Both gain-loss and gain-only trials were simultaneously fitted to the following Prospect-theory-inspired model [36]: where G is the gain (G>0), L is the loss (L<0 for gain-loss gambles and L = 0 for gain-only gambles), B the guaranteed gain (B = 0 for gain-loss gambles and B>0 for gain-only gambles), pG = 0.5 is the probability of a gain and pL = 1-pG = 0.5 is the probability of a loss. The free parameters of the model are: a) the loss aversion lambda (λ), i.e., the multiplicative weight associated with anticipated losses compared with gains; b) the risk aversion rho (ρ), i.e., the curvature of the value function u(x) = x^ρ that embodies the diminishing sensitivity to increasing outcome; and c) the choice consistency or “softmax temperature” (μ), i.e., a measure of noisiness vs. systematicity in choices. They were estimated via maximum likelihood estimation with MATLAB (MathWorks, Natick, MA) for each subject separately.

3. Results

3.1 Sociodemographic and clinical characteristics

Of 116 subjects who expressed an initial interest in the study, 40 refused (25 patients, 62.5%, and 15 healthy controls, 37.5%); we were unable to collect further data on these subjects due to constraints posed by the Ethical Committee.

Following previous studies assessing loss aversion based on mixed-gambles [4, 14, 36], inspection of the individual responses led us to exclude participants if the model did not converge, suggesting either ‘random choice’ behaviour or that they misunderstood the instructions, and when choices were suggestive of the tendency to accept or reject all gambles [47, 48]. Moreover, since the lack of a real financial incentive did not allow to interpret a loss-seeking pattern, we retained loss-neutral participants (lambda = 1) and excluded those with lambda<1.

We thereby removed 15, 11 and 3 participants for lack of model convergence, lambda <1 and lambda >8, respectively. Thus, the overall sample included 14 forensic and 21 non-forensic patients with SSD, and 41 healthy controls.

Table 1 shows the socio-demographic characteristics of both forensic and non-forensic patients and healthy controls. The majority of participants were males (N = 51; 67.1%), with a further male excess in the clinical group (forensic and non-forensic patients) compared to healthy controls (p<0.001).

thumbnail
Table 1. Socio–demographic characteristics of forensic patients with SSD, non–forensic patients with SSD and healthy controls.

https://doi.org/10.1371/journal.pone.0289152.t001

Compared to forensic and non-forensic patients with SSD, healthy controls were more frequently married or cohabiting (p = 0.001), had achieved a higher educational level (p<0.001) and were more often skilled or professional workers (<0.001). Moreover, forensic and non-forensic patients with SSD more often had a lifetime history of substance and alcohol misuse compared to healthy controls (p<0.001).

Descriptive statistics and between-groups comparisons regarding clinical characteristics in forensic and non-forensic patients are shown in Table 2. The most common diagnosis in both groups was schizophrenia (85.7%). Mean age at first contact with psychiatric services differed significantly between the two groups (p = 0.029), while the mean duration of illness was over 7 years in both groups. Forensic patients were more likely to meet criteria for a comorbid personality disorder than non-forensic patients (p = 0.006). There were no significant differences in current positive (p = 0.210) and negative (p = 0.881) symptoms, general psychopathology (p = 0.934) and PANSS total scores between the two patient groups (p = 0.778).

thumbnail
Table 2. Clinical characteristics of forensic patients with SSD and non–forensic patients with SSD.

https://doi.org/10.1371/journal.pone.0289152.t002

Forensic patients displayed better social functioning and lower level of disability, as assessed with the WHODAS (mean score: 1.6, SD = 2.4 for the forensic group vs mean score: 8.1, SD = 8.4 for the non-forensic one; p = 0.006).

Finally, forensic and non-forensic patients did not differ in terms of their neuro-cognitive parameters as assessed using the BACS.

3.2 Decision-making

There was a significant difference between the three groups in terms of risk aversion (p = 0.019). Post-hoc comparisons showed that this difference was driven by greater risk aversion among non-forensic patients with SSD compared to healthy controls (p = 0.020), with Cohen’s d = 0.69 suggesting a medium effect size. There were no significant differences among the three groups in loss aversion (p = 0.558) and choice consistency (p = 0.389) (Table 3).

thumbnail
Table 3. Decision–making experiment of forensic patients with SSD, non–forensic patients with SSD and healthy controls.

https://doi.org/10.1371/journal.pone.0289152.t003

These findings were also confirmed by multinomial logistic models adjusted for sex, lifetime substance/alcohol use and education (Table 4): although the corresponding odds ratios were not significant, risk aversion was the only significant predictor of membership of the three groups (p = 0.028) among the three decision-making variables investigated. This significant effect is due to the difference between the non-forensic group and healthy controls.

thumbnail
Table 4. Association between group and decision–making variables.

https://doi.org/10.1371/journal.pone.0289152.t004

4. Discussion

To the best of our knowledge, this is the first study which used well-established behavioural economics paradigms to compare loss and risk aversion across patients with SSD with and without a history of serious violence, and healthy participants. A multi-domain assessment of patients’ cognitive status was performed using the BACS, that was able to exclude group differences in cognition as contributing to differential decision-making performance.

There were no significant differences in any decision-making variables between forensic and non-forensic patients with SSD, while higher risk aversion was observed in non-forensic patients with SSD compared with healthy controls.

4.1 Risk aversion in people with SSD

This new evidence provides novel insights into a controversial literature showing both increased [31, 32] and decreased [33, 34] risk aversion in patients with SSD. Unlike some of these earlier studies, administering both gain-loss and gain-only trials allowed us to disentangle the effects of anticipating losses from that associated with risk in itself, resulting in a more specific assessment of risk aversion. This approach confirmed a more conservative decision-making in patients with SSD compared to healthy controls, which, alongside the lack of differences in loss aversion, suggests an impaired reward-based learning, with preserved punishment-based learning, in patients with SSD [31].

While our conclusions are limited by the small sample size, the present evidence of a significant difference in risk aversion suggests that our negative finding for differential loss aversion in SSD patients cannot be merely ascribed to power issues. Moreover, altered loss aversion in people with SSD is an issue for debate: previous related reports either found loss aversion to be absent in patients with SSD [34, 35] or, conversely, found no significant difference across patients and controls in this economic dimension [33]. Importantly, however, the studies reporting no differences in SSD inferred loss aversion from differential gain/loss scenarios within tasks assessing interpersonal coordination in a Prisoner’s dilemma [34] or price estimation in selling vs. buying conditions [35]. Both these experimental paradigms largely depart from those used in the psycho-economic literature, where individual differences in loss/punishment sensitivity are assessed through tasks that require a choice between accepting or rejecting mixed-gambles, thereby allowing direct tracking of the economic and affective weight placed on prospective losses [49, 50]. It is thus noteworthy that the present evidence of no significant differences between patients with SSD and healthy controls fits with that reported in the only previous study using mixed gambles to assess loss aversion in patients with SSD [33]. Overall, these findings suggest greater difficulties for SSD patients in implementing positive rather than negative feedback, when learning from past experiences.

In turn, this evidence suggests a new potential treatment target for rehabilitative measures aimed at achieving functional improvements in patients with SSD by selectively leveraging the neuro-cognitive processing of reward. Our results show that the greater risk aversion observed in patients with SSD is at least partially explained by education levels and past substance/alcohol use. While contributing to a controversial literature on the effects of alcohol intoxication [51, 52] and lifetime alcohol use [53, 54] on risk taking, these findings additionally suggest that socio-demographic considerations (such as the educational level or the marital status) should be evaluated when comparing the processing of risky outcomes across different populations.

4.2 Risk aversion in forensic and non-forensic patients with SSD

The lack of differences between forensic and non-forensic patients in our sample contributes to a controversial literature that has reported both greater risk-seeking levels [55], or normal adjustments of risk-taking to outcome probability [22, 23], in offenders. Previous studies reported alterations of typical “cool” executive functions (e.g., response-inhibition or planning) in this population, with no involvement of their “hot” (i.e., affect- or reward-related) counterpart, such as reversal-learning [21, 56]. The latter finding fits with previous evidence of comparable impulsivity and risk-taking in the Cambridge Gambling task [21]. By complementing these negative findings through a well-validated experimental paradigm, our results suggest that the cognitive alterations associated with forensic behaviour either involve cool executive functions (e.g., response inhibition) more than reward or risk valuations, or they are not properly captured by the decision-making tasks used in these studies. Indeed, the few studies reporting greater risk-taking in offenders have generally used the Iowa gambling task [57], which requires the coordinated activity of both hot and cool executive functions [57]. Moreover, the selective observation of altered risk aversion in non-forensic patients with SSD fits with recent evidence of greater risk aversion in this disorder, but not in SSD patients with anti-social personality disorders [32]. Altogether, these results might suggest that—if offenders’ forensic behaviour reflects alterations in specific valuation and decision-making processes–these might involve aspects other than loss or risk aversion, or that these economic dimensions should be assessed through choices involving other individuals’ welfare [58].

4.3 Limitations

Due to constraints posed both by the Ethical Committee and the specific treatment setting where the study took place (e.g., forensic facilities), we were not allowed to incentivize participants. This is clearly a limitation in a study on decision-making, particularly because it hampers interpreting values of lambda close to 1, i.e., those distinguishing among loss-averse, -neutral- and -seeker participants. This is a critical issue in the current literature on loss aversion, since the popular claim of an average λ≈215 has been questioned by the evidence of no loss aversion for small to moderate amounts [45, 46]. Based on the above considerations, we decided to exclude participants with lambda<1 (since their loss-seeking behaviour would not be interpretable in the lack or real losses), while retaining those will lambda = 1 (and thus accommodating a loss-neutral pattern). The lack of real financial outcomes might have thus biased the present findings, which are therefore in need of replications by future studies with larger samples and a more ecological incentivization procedure.

5. Conclusions

This is the first study to compare patients with SSD with and without a history of serious violence, and healthy controls, in a well-validated risk-taking behavioural paradigm. Recruiting non-forensic patients with SSD as a primary control group allowed us to better unpick the effects of mental disorders and other clinically-relevant factors which might otherwise contribute to seemingly antisocial behaviour. Despite the lack of significant evidence for selective neuro-cognitive markers of offending, we identified aspects of decision-making under risk which might prove useful for assessing altered high-order executive functioning in people with SSD. While further studies are required to investigate whether, and to what extent, such alterations might also help explain antisocial behaviours, such as those displayed by forensic sample, these findings highlight specific target cognitive domains for treatment and rehabilitation in patients with SSD.

Supporting information

S2 File. Questionnaire on risk factors for the index violence–Q.

https://doi.org/10.1371/journal.pone.0289152.s002

(DOCX)

S3 File. Full instructions of the risk aversion task.

https://doi.org/10.1371/journal.pone.0289152.s003

(DOCX)

S4 File. Full instructions of the loss aversion task.

https://doi.org/10.1371/journal.pone.0289152.s004

(DOCX)

Acknowledgments

Collaborators: R. Oberndorfer, A. Reisegger, T. Stompe, (Clinical Division of Social Psychiatry, Department of Psychiatry and Psychotherapy, Medical University of Vienna, Austria); B. Horten, A. Giersiefen, J. Schmidt (Central Institute of Mental Health, Mannheim, Germany); R. Ruiz (Institute of Psychiatry, Psychology and Neuroscience, King’s College London); M. Ozimkowicz, M. Pacholski (Institute of Psychiatry and Neurology, Warsaw).

Acknowledgments are also due to: Austria: M. Koch, S. Stadtmann, A. Unger, H. Winkler (Clinical Division of Social Psychiatry, Department of Psychiatry and Psychotherapy, Medical University of Vienna, Austria), A. Dvorak (Justinzanstalt Goellersdorf, Goellersdorf, Austria), A. Kastner (Klinik für Psychiatrie mit forensischem Schwerpunkt, Linz, Austria). Germany: H. Dressing, E. Biebinger (Klinik für Forensische Psychiatrie Klingenmünster), C. Oberbauer (Klinik für Forensische Psychiatrie und Psychotherapie Wiesloch), M. Michel (Klinik für Forensische Psychiatrie und Psychotherapie Weinsberg). Italy: G. Tura, A. Adorni, S. Bignotti, L. Rillosi, G. Rossi (IRCCS Fatebenefratelli, Brescia), F. Franconi, I. Rossetto, A.Cicolini (REMS ASST Mantova, Italy), C. Piazza (REMS ULSS9 Scaligera, Verona, Italy), F. Lazzerini (REMS AUSL Toscana Nord-Ovest), C. Villella, G. Alocci (REMS ASL Roma 5), A. Vita, P. Cacciani, A. Galluzzo (Department of Mental Health, ASST Spedali Civili, Brescia). Poland: A. Pilszyk, P. Gosek (Institute of Psychiatry and Neurology, Warsaw), A. Welento-Nowacka (Forensic Department, Mental Health Hospital in Starogard Gdański). United Kingdom: N. Blackwood (Institute of Psychiatry, Psychology and Neuroscience, King’s College London). Thanks are also due to Anja Vaskinn (Centre for Research and Education in Forensic Psychiatry, Oslo University Hospital; Norwegian Centre for Mental Disorders Research, Institute of Clinical Medicine, University of Oslo), who provided valuable comments.

References

  1. 1. Liu X, Hairston J, Schrier M, Fan J. Common and distinct networks underlying reward valence and processing stages: a meta-analysis of functional neuroimaging studies. Neurosci Biobehav Rev 2011 Apr;35(5):1219–1236.
  2. 2. Pessiglione M, Delgado MR. The good, the bad and the brain: Neural correlates of appetitive and aversive values underlying decision making. Curr Opin Behav Sci 2015 Oct;5:78–84. pmid:31179377
  3. 3. Canessa N, Crespi C, Baud-Bovy G, Dodich A, Falini A, Antonellis G, et al. Neural markers of loss aversion in resting-state brain activity. Neuroimage 2017 Feb 1;146:257–265. pmid:27884798
  4. 4. Canessa N, Crespi C, Motterlini M, Baud-Bovy G, Chierchia G, Pantaleo G, et al. The functional and structural neural basis of individual differences in loss aversion. J Neurosci 2013 Sep 4;33(36):14307–14317. pmid:24005284
  5. 5. Arioli M, Cattaneo Z, Parimbelli S, Canessa N. Relational vs representational social cognitive processing: a coordinate-based meta-analysis of neuroimaging data. Soc Cogn Affect Neurosci. 2023;18(1):nsad003. pmid:36695428
  6. 6. Ridderinkhof KR, Ullsperger M, Crone EA, Nieuwenhuis S. The role of the medial frontal cortex in cognitive control. Science 2004 Oct 15;306(5695):443–447. pmid:15486290
  7. 7. Beszterczey S, Nestor PG, Shirai A, Harding S. Neuropsychology of decision making and psychopathy in high-risk ex-offenders. Neuropsychology 2013 Jul;27(4):491–497. pmid:23876121
  8. 8. Ernst M, Paulus MP. Neurobiology of decision making: a selective review from a neurocognitive and clinical perspective. Biol Psychiatry 2005 Oct 15;58(8):597–604. pmid:16095567
  9. 9. Shenhav A, Botvinick MM, Cohen JD. The expected value of control: an integrative theory of anterior cingulate cortex function. Neuron 2013 Jul 24;79(2):217–240. pmid:23889930
  10. 10. Kahneman D, Tversky A. Choices, values, and frames. American Psychologist 1984;39(4):341–350.
  11. 11. Sokol-Hessner P, Lackovic SF, Tobe RH, Camerer CF, Leventhal BL, Phelps EA. Determinants of Propranolol’s Selective Effect on Loss Aversion. Psychol Sci 2015 Jul;26(7):1123–1130. pmid:26063441
  12. 12. Lopez-Guzman S, Konova AB, Glimcher PW. Computational psychiatry of impulsivity and risk: how risk and time preferences interact in health and disease. Philos Trans R Soc Lond B Biol Sci 2019 Feb 18;374(1766):20180135. pmid:30966919
  13. 13. De Martino B, Kumaran D, Seymour B, Dolan RJ. Frames, biases, and rational decision-making in the human brain. Science 2006 Aug 4;313(5787):684–687. pmid:16888142
  14. 14. Tom SM, Fox CR, Trepel C, Poldrack RA. The neural basis of loss aversion in decision-making under risk. Science 2007 Jan 26;315(5811):515–518. pmid:17255512
  15. 15. Yechiam E, Kanz JE, Bechara A, Stout JC, Busemeyer JR, Altmaier EM, et al. Neurocognitive deficits related to poor decision making in people behind bars. Psychon Bull Rev 2008 Feb;15(1):44–51. pmid:18605478
  16. 16. Cohen LE, Felson M. Social Change and Crime Rate Trends: A Routine Activity Approach. American Sociological Review 1979;44(4):588–608.
  17. 17. Cornish DB, Clarke RV. Understanding crime displacement: an application of rational choice theory. Criminology 1987;25:933–948.
  18. 18. Cornish DB, Clarke RV. The reasoning criminal rational choice perspectives on offending. Routledge (2014).
  19. 19. Fazel S, Hayes AJ, Bartellas K, Clerici M, Trestman R. Mental health of prisoners: prevalence, adverse outcomes, and interventions. Lancet Psychiatry 2016 Sep;3(9):871–881.
  20. 20. Fazel S, Seewald K. Severe mental illness in 33,588 prisoners worldwide: systematic review and meta-regression analysis. Br J Psychiatry 2012 May;200(5):364–373. pmid:22550330
  21. 21. De Brito SA, Viding E, Kumari V, Blackwood N, Hodgins S. Cool and hot executive function impairments in violent offenders with antisocial personality disorder with and without psychopathy. PLoS One 2013 Jun 20;8(6):e65566. pmid:23840340
  22. 22. Grogger J. Certainty vs. severity of punishment. Economic Inquiry 1991;29:297–309.
  23. 23. Block MK, Gerety VE. Some Experimental Evidence on Differences between Student and Prisoner Reactions to Monetary Penalties and Risk. The Journal of Legal Studies 1995;24.
  24. 24. Jones KA, Hewson T, Sales CP, Khalifa N. A Systematic Review and Meta-Analysis of Decision-Making in Offender Populations with Mental Disorder. Neuropsychol Rev 2019 Jun;29(2):244–258. pmid:30798419
  25. 25. Umbach R, Leonard NR, Luciana M, Ling S, Laitner C. The Iowa Gambling Task in Violent and Nonviolent Incarcerated Male Adolescents. Crim Justice Behav 2019 Nov 1;46(11):1611–1629. pmid:32981980
  26. 26. Hiser J, Koenigs M. The Multifaceted Role of the Ventromedial Prefrontal Cortex in Emotion, Decision Making, Social Cognition, and Psychopathology. Biol Psychiatry 2018 Apr 15;83(8):638–647. pmid:29275839
  27. 27. Sevy S, Burdick KE, Visweswaraiah H, Abdelmessih S, Lukin M, Yechiam E, et al. Iowa gambling task in schizophrenia: a review and new data in patients with schizophrenia and co-occurring cannabis use disorders. Schizophr Res 2007 May;92(1–3):74–84. pmid:17379482
  28. 28. Woodrow A, Sparks S, Bobrovskaia V, Paterson C, Murphy P, Hutton P. Decision-making ability in psychosis: a systematic review and meta-analysis of the magnitude, specificity and correlates of impaired performance on the Iowa and Cambridge Gambling Tasks. Psychol Med 2019 Jan;49(1):32–48. pmid:30246669
  29. 29. Kester HM, Sevy S, Yechiam E, Burdick KE, Cervellione KL, Kumra S. Decision-making impairments in adolescents with early-onset schizophrenia. Schizophr Res 2006 Jul;85(1–3):113–123. pmid:16733084
  30. 30. Pedersen A, Göder R, Tomczyk S, Ohrmann P. Risky decision-making under risk in schizophrenia: A deliberate choice? J Behav Ther Exp Psychiatry 2017 Sep;56:57–64. pmid:27568887
  31. 31. Msk L, Wc C, Csy C, Cmw S, Skw C, Emh L, et al. Altered risky decision making in patients with early non-affective psychosis. Eur Arch Psychiatry Clin Neurosci 2021 Jun;271(4):723–731. pmid:30806772
  32. 32. Sabater-Grande G, Haro G, García-Gallego A, Georgantzís N, Herranz-Zarzoso N, Baquero A. Risk-taking and fairness among cocaine-dependent patients in dual diagnoses: Schizophrenia and Anti-Social Personality Disorder. Sci Rep 2020 Jun 22;10(1):10120-020-66954-2. pmid:32572083
  33. 33. Brown JK, Waltz JA, Strauss GP, McMahon RP, Frank MJ, Gold JM. Hypothetical decision making in schizophrenia: the role of expected value computation and "irrational" biases. Psychiatry Res 2013 Sep 30;209(2):142–149. pmid:23664664
  34. 34. Currie J, Buruju D, Perrin JS, Reid IC, Steele JD, Feltovich N. Schizophrenia illness severity is associated with reduced loss aversion. Brain Res 2017 Jun 1;1664:9–16. pmid:28288869
  35. 35. Trémeau F, Brady M, Saccente E, Moreno A, Epstein H, Citrome L, et al. Loss aversion in schizophrenia. Schizophr Res 2008 Aug;103(1–3):121–128. pmid:18501565
  36. 36. Sokol-Hessner P, Camerer CF, Phelps EA. Emotion regulation reduces loss aversion and decreases amygdala responses to losses. Soc Cogn Affect Neurosci 2013 Mar;8(3):341–350. pmid:22275168
  37. 37. Klaus F, Chumbley JR, Seifritz E, Kaiser S, Hartmann-Riemer M. Loss Aversion and Risk Aversion in Non-Clinical Negative Symptoms and Hypomania. Front Psychiatry 2020 Sep 23;11:574131. pmid:33173521
  38. 38. de Girolamo G, Iozzino L, Ferrari C, et al. A multinational case-control study comparing forensic and non-forensic patients with schizophrenia spectrum disorders: the EU-VIORMED project [published online ahead of print, 2021 Sep 13]. Psychol Med. 2021:1–11 (2021).
  39. 39. American Psychiatric Association. Diagnostic and statistical manual of mental disorders (fifth ed.). Arlington V.A. (American Psychiatric Publishing; 2013. p. 5–25. ISBN 978-0-89042-555-8).
  40. 40. Kay SR, Fiszbein A, Opler LA. The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophr Bull 1987;13(2):261–276. pmid:3616518
  41. 41. Langeveld J, Andreassen OA, Auestad B, Færden A, Hauge LJ, Joa I, et al. Is there an optimal factor structure of the Positive and Negative Syndrome Scale in patients with first-episode psychosis? Scand J Psychol 2013 Apr;54(2):160–165. pmid:23252448
  42. 42. Wallwork RS, Fortgang R, Hashimoto R, Weinberger DR, Dickinson D. Searching for a consensus five-factor model of the Positive and Negative Syndrome Scale for schizophrenia. Schizophr Res 2012 May;137(1–3):246–250. pmid:22356801
  43. 43. Keefe RS, Goldberg TE, Harvey PD, Gold JM, Poe MP, Coughenour L. The Brief Assessment of Cognition in Schizophrenia: reliability, sensitivity, and comparison with a standard neurocognitive battery. Schizophr Res 2004 Jun 1;68(2–3):283–297. pmid:15099610
  44. 44. Ustün TB, Chatterji S, Kostanjsek N, Rehm J, Kennedy C, Epping-Jordan J, et al. Developing the World Health Organization Disability Assessment Schedule 2.0. Bull World Health Organ 2010 Nov 1;88(11):815–823. pmid:21076562
  45. 45. Yechiam E, Hochman G. Loss-aversion or loss-attention: the impact of losses on cognitive performance. Cogn Psychol 2013 Mar;66(2):212–231. pmid:23334108
  46. 46. Yechiam E, Zeif D. The effect of methylphenidate and mixed amphetamine salts on cognitive reflection: a field study. Psychopharmacology (Berl) 2022 Feb;239(2):455–463. pmid:34729642
  47. 47. Chiong W, Wood KA, Beagle AJ, Hsu M, Kayser AS, Miller BL, et al. Neuroeconomic dissociation of semantic dementia and behavioural variant frontotemporal dementia. Brain 2016 Feb;139(Pt 2):578–587. pmid:26667277
  48. 48. Ligneul R, Sescousse G, Barbalat G, Domenech P, Dreher JC. Shifted risk preferences in pathological gambling. Psychol Med 2013 May;43(5):1059–1068. pmid:22932231
  49. 49. Strickland JC, Beckmann JS, Rush CR, Stoops WW. A pilot study of loss aversion for drug and non-drug commodities in cocaine users. Drug Alcohol Depend 2017 Nov 1;180:223–226. pmid:28922652
  50. 50. Sokol-Hessner P, Hartley CA, Hamilton JR, Phelps EA. Interoceptive ability predicts aversion to losses. Cogn Emot 2015;29(4):695–701. pmid:24916358
  51. 51. Burghart DR, Glimcher PW, Lazzaro SC. An expected utility maximizer walks into a bar…. J Risk Uncertain 2013 Jun;46(3):10.1007/s11166-013-9167-7. pmid:24244072
  52. 52. Proestakis A., Espín A. M., Exadaktylos F., Cortés Aguilar A., Oyediran O. A., & Palacio L. A. The separate effects of self-estimated and actual alcohol intoxication on risk taking: A field experiment. Journal of Neuroscience, Psychology, and Economics 6(2), 115–135 (2013).
  53. 53. Anderson LR, Mellor JM. Predicting health behaviors with an experimental measure of risk preference. J Health Econ 2008 Sep;27(5):1260–1274. pmid:18621427
  54. 54. Barsky RB, Juster FT, Kimball MS, Shapiro MD. Preference Parameters and Behavioral Heterogeneity: An Experimental Approach in the Health and Retirement Study. The Quarterly Journal of Economics 1997;112(2):537–579.
  55. 55. Becker GS. Crime and Punishment: An Economic Approach. Journal of Political Economy 1968;76(2):169–217.
  56. 56. Dolan M. The neuropsychology of prefrontal function in antisocial personality disordered offenders with varying degrees of psychopathy. Psychol Med 2012 Aug;42(8):1715–1725. pmid:22142550
  57. 57. Dunn BD, Dalgleish T, Lawrence AD. The somatic marker hypothesis: a critical evaluation. Neurosci Biobehav Rev 2006;30(2):239–271. pmid:16197997
  58. 58. Arioli M, Basso G, Baud-Bovy G, Mattioni L, Poggi P, Canessa N. Neural bases of loss aversion when choosing for oneself versus known or unknown others. Cerebral Cortex 2023;33(11):7120–7135. pmid:36748997